Pharmacovigilance
Drug safety starts with every report
If you experience or observe a suspected adverse event involving a medicinal product manufactured by Suyaash Pharmaceuticals, please tell our Pharmacovigilance team. Your report can help us monitor product safety and protect patients.
Download the form
Open the PDF form and save or print a copy.
Add the details
Complete as much information as you can. You may still report when some details are unavailable.
Email your report
Attach the completed form and relevant supporting documents to your email.
What is an adverse event?
An adverse event is an unwanted or unexpected medical occurrence that happens while a person is using a medicinal product. A report does not need to prove that the product caused the event.
Who can report?
Patients, caregivers, doctors, pharmacists and other healthcare professionals may submit a report.
What should you include?
- Patient details that help identify the case without unnecessary personal information
- Product name, strength, batch number and how it was used
- A description of the event, relevant dates and outcome
- Your contact information so the team can request follow-up details
Why report?
Every report adds to the safety information available for a product. It helps the Pharmacovigilance team review patterns, request follow-up information and take appropriate action when needed.
Submit your report
Download the form, complete it and email it to the Suyaash Pharmaceuticals Pharmacovigilance team. You can also include prescriptions, laboratory results or discharge summaries that are relevant to the event.
Privacy and confidentiality
Information is requested to assess and follow up the reported safety concern. Personal information will be handled confidentially for pharmacovigilance and applicable reporting responsibilities.